Principal Job Responsibilities:
· Develop, conduct and lead clinical trial projects
· Participate and/or lead implementation of on-going clinical researches through handling clinical activities such as recruitment, screening, enrolment and follow-up of research participants.
· Lead and provide medical care to study participants as necessary
· Participate with CTD and beyond team in problem identification for research, research designing, research protocol development, data collection, analysis, interpretation and report writing.
· Prepare and/or lead grant writing independently and/or in collaboration with senior and junior researchers in the respective Directorates.
· Conduct and lead clinical examinations and medical follow-up of study participants.
· Conduct and coordinate other clinical procedures required in a study protocol.
· Conduct and/or Lead data collection, CRF completion, verify and review clinical data
· Lead and provide counselling and medical care of study participants as a physician.
· Ensure protection, care and retention of study participants during a study conduct.
· Follow-up, recording & reporting of AEs, NEs & SAEs as deemed necessary.
· Prepare clinical and project progress report.
· Cooperate in ensuring quality control activities in the conduct of trials.
· Representing the directorate/institute in any scientific platforms for paper presentation and/or participation when applicable
· Perform miscellaneous job-related duties as assigned by the director and/or the principal investigator.
Specifications for the Position:
Qualification, Experiences and Essential Skills
- MD plus speciality certificate in Paediatrics with min 6 years of experience in medical practice as paediatrician; plus
- Experience in clinical research and scientific paper writing with at least two publication points (at least one publication as first author) is mandatory.
- Experience in clinical trial at the position of Principal Investigator is given priority.